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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 126774Generated: October 31, 2026

1-Carbethoxycarbonylmethyl-2-amino-3-carbamoyl-quinoxalinium bromide → Ethyl 4-carbamoyl-imidazo-[1,2-a]-quinoxaline-2-carboxylate

https://huagongshe.com/reaction/126774

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Carbethoxycarbonylmethyl-2-amino-3-carbamoyl-quinoxalinium bromideHCID 20287983—
SolventEthanolHCID 702—
ProductEthyl 4-carbamoyl-imidazo-[1,2-a]-quinoxaline-2-carboxylateHCID 1406752174.1%

Reaction Steps

A suspension of 1 g of the product of Step A in 100 ml of ethanol was refluxed with stirring for 90 minutes and the resulting yellow solution was concentrated and cooled. The mixture was filtered to obtain 0.55 g of ethyl 4-carbamoyl-imidazo-[1,2-a]-quinoxaline-2-carboxylate as a pale yellow crystalline solid. Recrystallization from ethanol yielded soft white needles melting at 280°-284° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04254123
Source datasetuspto-grants-1981_03
ORD IDord-f314d70b542d41eeba794cd016ca4891
Source noteuspto-grants-1981_03